Nothing Special   »   [go: up one dir, main page]

EP0751869A1 - Release sheet - Google Patents

Release sheet

Info

Publication number
EP0751869A1
EP0751869A1 EP95910316A EP95910316A EP0751869A1 EP 0751869 A1 EP0751869 A1 EP 0751869A1 EP 95910316 A EP95910316 A EP 95910316A EP 95910316 A EP95910316 A EP 95910316A EP 0751869 A1 EP0751869 A1 EP 0751869A1
Authority
EP
European Patent Office
Prior art keywords
acrylate
release
silicone
flexible sheet
carboxylate groups
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP95910316A
Other languages
German (de)
French (fr)
Other versions
EP0751869A4 (en
Inventor
Pang Chia Lu
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Oil Corp
Original Assignee
Mobil Oil Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mobil Oil Corp filed Critical Mobil Oil Corp
Publication of EP0751869A1 publication Critical patent/EP0751869A1/en
Publication of EP0751869A4 publication Critical patent/EP0751869A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/201Adhesives in the form of films or foils characterised by their carriers characterised by the release coating composition on the carrier layer
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/40Adhesives in the form of films or foils characterised by release liners
    • C09J7/401Adhesives in the form of films or foils characterised by release liners characterised by the release coating composition
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/40Adhesives in the form of films or foils characterised by release liners
    • C09J7/405Adhesives in the form of films or foils characterised by release liners characterised by the substrate of the release liner
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/40Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/414Additional features of adhesives in the form of films or foils characterized by the presence of essential components presence of a copolymer
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/40Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/416Additional features of adhesives in the form of films or foils characterized by the presence of essential components use of irradiation
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2400/00Presence of inorganic and organic materials
    • C09J2400/20Presence of organic materials
    • C09J2400/28Presence of paper
    • C09J2400/283Presence of paper in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2423/00Presence of polyolefin
    • C09J2423/04Presence of homo or copolymers of ethene
    • C09J2423/046Presence of homo or copolymers of ethene in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2423/00Presence of polyolefin
    • C09J2423/10Presence of homo or copolymers of propene
    • C09J2423/106Presence of homo or copolymers of propene in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2425/00Presence of styrenic polymer
    • C09J2425/006Presence of styrenic polymer in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2433/00Presence of (meth)acrylic polymer
    • C09J2433/005Presence of (meth)acrylic polymer in the release coating
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2467/00Presence of polyester
    • C09J2467/006Presence of polyester in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2477/00Presence of polyamide
    • C09J2477/006Presence of polyamide in the substrate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2483/00Presence of polysiloxane
    • C09J2483/005Presence of polysiloxane in the release coating
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/14Layer or component removable to expose adhesive
    • Y10T428/1462Polymer derived from material having at least one acrylic or alkacrylic group or the nitrile or amide derivative thereof [e.g., acrylamide, acrylate ester, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2809Web or sheet containing structurally defined element or component and having an adhesive outermost layer including irradiated or wave energy treated component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2839Web or sheet containing structurally defined element or component and having an adhesive outermost layer with release or antistick coating
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31652Of asbestos
    • Y10T428/31663As siloxane, silicone or silane
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31652Of asbestos
    • Y10T428/31667Next to addition polymer from unsaturated monomers, or aldehyde or ketone condensation product

Definitions

  • the invention relates to a composite film suitable for use as a release sheet. It more specifically relates to composite films which are suitable for high speed label dispensing machines.
  • Peelable labels are well known. They are constructed from a release liner upon which there is a release coating, an adhesive and a face stock. The face stock is releasably adhered to the release liner by contact with an adhesive located between the face stock and the release liner.
  • the release liner is constructed by applying a release coating to one side of a plastic or paper liner sheet.
  • Release coatings are characterized by an ability to adhere strongly to the liner sheet but to adhere weakly to the adhesive which is located between the face stock and the liner.
  • the peelable label is converted into roll label stock by cutting the composite film with a die which only cuts through the face stock, not through the release liner, to form labels of specified shape.
  • the surrounding face stock known as the matrix, is stripped away from the release liner, leaving the labels adhered to the release liner which is then formed into a roll.
  • the labels are usually dispensed by bending the roll stock to an angle which causes the label to lift away from the release liner.
  • the label, released from the liner is then applied to a surface.
  • the release coating is usually made out of an electron beam curable composition which, typically includes a silicone resin having crosslinkable groups, such as acrylic residues.
  • the silicone portion of the composition is the release agent which permits the adhesive to bond lightly to the release liner.
  • the acrylic groups crosslink the release coating composition together and permit the release coating to form a strong bond to the surface of the liner sheet.
  • release force typically four levels of release force: premium release (10 to 15 g) , easy release (20 to 40 g) , high release (50 to lOOg) and tight release (>100 g) .
  • the release liner should have a high release force. If the release force is too low, pre-dispensing occurs in which the labels disengage during die cutting rather than remain on the liner to form the roll stock.
  • Zippy noise is an art-recognized term used to describe a jerking noise generated during the high speed matrix stripping process.
  • This invention seeks to provide a release coating for use in high speed label dispensing machinery which does not cause pre-dispensing problems; for example, an unacceptable degree of zippy noise.
  • a feature of the invention is a release coating formulation which includes a mixture of (a) a silicone release component, (b) a crosslinking agent and (c) an acrylic ester.
  • a flexible sheet suitably but not exclusively for use as a release coated refuse liner, which has one one side thereof a crosslinkable release coating comprising a mixture of
  • a crosslinking agent differing from (a) , comprising a plurality of unsaturated carboxylate groups; and (c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) .
  • This invention also provides a crosslinkable release coating composition which comprises :
  • a crosslinking agent differing from (a) , comprising a plurality of unsaturated carboxylate groups;
  • This invention further provides a peelable adhesive film, for example a peelable label, which comprises a flexible sheet according to the invention and a face film stock releasably adhered by a tacky adhesive to the cured release coating.
  • a peelable adhesive film for example a peelable label, which comprises a flexible sheet according to the invention and a face film stock releasably adhered by a tacky adhesive to the cured release coating.
  • the present invention provides the use in a crosslinkable release coating composition which comprises :
  • a crosslinking agent differing from (a) , comprising a plurality of unsaturated carboxylate groups; and of (c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) to reduce pre-dispensing problems in high speed labelling.
  • An important feature of the invention is the use of a monomeric of oligomeric unsaturated carboxylic ester, preferably an acrylic ester in the release coating formulation.
  • Suitable such acrylic esters are monomers or oligomers having long chain hydrocarbon groups.
  • the hydrocarbon groups usually comprise 2 to 24 carbon atoms, specifically from 4 to 12 carbon atoms.
  • Specific examples of contemplated acrylic esters include octyl acrylate, isodecyl acrylate, stearyl acrylate and lauryl acrylate. These materials have viscosity ranges from 2 to 55 cP (2 mPas to 55 mPas) at 25°C.
  • the film form liner is a conventional flexible film material known in this art.
  • useful film form liner materials include paper, oriented polypropylene, polyethylene terephthalate, polyethylene, polyamides and polystyrene.
  • the release coating is a composition which when applied to the base liner, has a low surface tack permitting ready release of other materials such as polymeric films which have been applied thereto.
  • the release coating formulation of this invention is, typically, crosslinkable and comprises a mixture of (a) a silicone release component; (b) a crosslinking agent; and (c) an acrylic ester.
  • the (a) silicone release component is a polydimethyl siloxane silicone polymer which is known to have release characteristics.
  • the silicone polymers are themselves crosslinkable and have crosslinkable groups.
  • Crosslinkable silicone polymers of this kind usually have appended acrylic residues which are the crosslinkable groups. These crosslinkable silicone release polymers typically contain from 2%, such as 5%, to 30% acrylate, specifically from 10% to about 20% acrylate.
  • An example of a typical release coating is a silicone-acrylate copolymer described in EPA 0281681.
  • An example of a useful silicone-acrylate release polymer is available commercially under the name RC-726 by Goldschmidt Chemical Co.
  • the (b) crosslinking agent is present to permit bonding of the (a) silicone release component to the base liner.
  • the crosslinking agent interacts with the acrylate by free radical reactions, typically, induced by high energy radiation, e.g. electron beam or ultra violet light.
  • Conventional crosslinking agents can be employed in the release coating formulation.
  • An example of a contemplated crosslinking agent is a higher acrylate content silicone-acrylate.
  • the high acrylate content silicone-acrylate contemplated as the crosslinking agent is distinguished from the (a) silicone- acrylate by the presence of a higher concentration of the acrylate component.
  • the (b) silicone-acrylate contains from 5 to 15% more acrylate than the (a) silicone- acrylate.
  • the high acrylate silicone-acrylate contains from 10% to 45%, more specifically from 15% to 30% acrylate based on the entire weight of this crosslinking agent.
  • a high acrylate silicone-acrylate material which contains about
  • 25 % acrylate is sold commercially under the name RC-705 by Goldschmidt Chemical Co.
  • crosslinking agents are multi- functionalized acrylate monomer/oligomer materials.
  • Multi- functionalized acrylates are usually characterized by the presence of 2 or more acrylate groups per molecule. Examples include tri ethylolpropane triacrylate (TMPTA) and ethoxylated trimethylolpropane triacrylate (EO-TMPTA) .
  • TMPTA tri ethylolpropane triacrylate
  • EO-TMPTA ethoxylated trimethylolpropane triacrylate
  • the TMPTA is sold under the name "SR-351" and the EO-TMPTA is sold under the name "SR-454", both sold by Sartomer Chemical Co. of Exton, PA.
  • the TMPTA and/or EO-TMPTA can be used together with the high acrylate silicone-acrylate crosslinking agent to make-up the appropriate amount of crosslinker needed in the release coating.
  • the TMPTA and/or EO-TMPTA or the high acrylate silicone-acrylate can be used alone.
  • An important feature of this invention is the presence of a (c) acrylic ester in the release coating.
  • the (c) acrylic ester when used with (a) and (b) to form a release coating has been found to produce a high release force release coating material.
  • the (c) acrylic ester permits the above described (a) silicone release component to be used in high speed, high release force label applications.
  • easy release force release coatings made from (a) silicone release components were unusable in high release force applications. It is believed that the addition of the (c) acrylic ester modifies the elastic property of the crosslinked silicone release coating.
  • Contemplated acrylic esters include monomeric and/or oligomeric acrylates.
  • the acrylic esters contemplated are distinguished from the (a) and (b) silicone-acrylates described above by the absence of the silicone component. They are also distinguished from the (b) non-silicone crosslinking agent because they are usually free of more than two acrylate groups. Thus, more specifically, the acrylic ester can be defined as being free of silicone and free of more than 2 acrylate groups per molecule.
  • Acrylic esters are derivatives of both acrylic acid and ethacrylic acid.
  • the contemplated acrylates are specifically long chain alkyl esters containing 2 to 24 carbon atoms, the alkyl groups can be n-alkyl and secondary and branched chain alkyl groups.
  • acrylic esters include octyl acrylate, isodecyl acrylate, stearyl acrylate and lauryl acrylate. Typically the acrylic esters have viscosity ranges from 2 to 55 cP at 25°C (2 mPas to 55 mPas) . These acrylic esters are commercially available from several chemical companies, such as Sartomer, UCB Radcure and CPS Chemicals.
  • the release coating formulation is usually disposed on the base liner in an uncured from and is then cured to fix it in place.
  • the crosslinked release coating contains mostly crosslinked silicone acrylate moieties which are bound together and to the surface of the base liner.
  • the coating can also be crosslinked by adding a UV initiator and then exposing the coating to UV light. Typical UV initiators are hydroquinone and hydroquinone derivatives.
  • the face stock is a conventional film form material.
  • suitable materials are films of paper, oriented polypropylene, polyethylene terephthalate, polyethylene, polystyrene and metal foils.
  • the adhesive is any material which will bond weakly to the release liner and strongly to the face stock.
  • known adhesives include acrylic emulsions, such as those sold commercially under the name XPLA-12, by the Dyna-tech Company, styrene-butadiene rubber emulsions, such as those sold under the name Bond-master 72-9718 by National Starch Company, and hot- melt adhesives, such as those sold under the trade name HL-2021, or HL-2203X by the H.B. Fuller Company.
  • a base liner provided with a skin of a material having tougher physical properties, adjacent to the release coating.
  • This base liner is designed to facilitate label cutting.
  • the proportion of each component described above in the release coating formulation ranges from 15 to 70%, specifically from 20 to 50%, of the (a) silicone release component; from 10% to 50%, specifically from 15% to 30% of the (b) crosslinking agent; and from 10% to 50%, specifically from 20% to 40% of the (c) acrylic ester.
  • the following Examples illustrate the invention; parts and percentages are by weight unless expressly stated.
  • a release coating was formulated from a curable silicone- acrylate release component (RC-726 manufactured by Goldschmidt Chemical Co.), various proportions of the crosslinking agents, ethoxylated trimethylolpropane triacrylate (EO-TMPTA) and high acrylate silicone acrylate (HASA) , and isodecyl acrylate.
  • the formulated release coating was coated onto a 2.0 mil oriented polypropylene film. After application of the release coating, the film was radiation cured by exposure to 2.5 Mrad electron beam radiation on an ESI Electrocurtain CB 150 laboratory EB unit. The release force of each coated release liner was tested by a TLMI tester.
  • the TLMI tester is manufactured by TMI Co. , of Amityville, NY.
  • the sandwich laminate is cut into a 1 inch (25.4 mm) width.
  • the face stock is peeled away at a 180° angle at a speed of 300 in/minute (1,270 mm/s) .
  • the peel force is reported as the release force.
  • the results are reported below in Table 1.
  • the release liners were laminated to a high release force adhesive tape.
  • the peel force at a speed of 3 and 5 meters per second was measured with IMASS tester.
  • the IMASS tester is used to measure the release force for high speed operation.
  • the tester used was model ZPE-1000, manufactured by Instrumentors, Inc., Strongsville OH which can be operated at speeds of 0.5 to 5.0 meters per second.
  • the results are reported in Table 1.
  • EO-TMPTA Ethoxylated Trimethylolpropane Triacrylate
  • Samples 1 to 8 were laminated to 60# high gloss paper face stock with a hot melt adhesive on a laboratory Mercer laminator. The laminates were then evaluated for their die cut performance on the Allied Gear FlexmasterlB die cut machine with a 3/4" circular die and the results are reported in Table 2. The percent predispense was determined by counting the number of labels predispensed during matrix stripping at 200 fpm (60.96 m/min) and 500 fpm (152.40 m/min) . TABLE 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesive Tapes (AREA)
  • Laminated Bodies (AREA)

Abstract

A composite sheet of a flexible release liner, which is useful in high speed operations, the release liner is coated on one side with a crosslinkable high release coating formulation comprising (a) a silicone-acrylate release component; (b) an acrylate-containing crosslinking agent, such as a silicon-acrylate crosslinking agent having a higher acrylate content than the (a) silicone-acrylate, trimethylolpropane triacrylate or epoxylated trimethylolpropane triacrylate; and (c) an acrylic ester monomer or oligomer selected from the group consisting of octyl acrylate, isodecyl acrylate, stearyl acrylate and lauryl acrylate, specifically the (c) acrylate is free of silicone and more than two acrylate groups per molecule.

Description

RELEASE SHEET
The invention relates to a composite film suitable for use as a release sheet. It more specifically relates to composite films which are suitable for high speed label dispensing machines.
Peelable labels are well known. They are constructed from a release liner upon which there is a release coating, an adhesive and a face stock. The face stock is releasably adhered to the release liner by contact with an adhesive located between the face stock and the release liner.
Typically the release liner is constructed by applying a release coating to one side of a plastic or paper liner sheet.
Release coatings are characterized by an ability to adhere strongly to the liner sheet but to adhere weakly to the adhesive which is located between the face stock and the liner.
The peelable label is converted into roll label stock by cutting the composite film with a die which only cuts through the face stock, not through the release liner, to form labels of specified shape. The surrounding face stock, known as the matrix, is stripped away from the release liner, leaving the labels adhered to the release liner which is then formed into a roll. The labels are usually dispensed by bending the roll stock to an angle which causes the label to lift away from the release liner. The label, released from the liner, is then applied to a surface.
In composite films of this type, the release coating is usually made out of an electron beam curable composition which, typically includes a silicone resin having crosslinkable groups, such as acrylic residues. The silicone portion of the composition is the release agent which permits the adhesive to bond lightly to the release liner. The acrylic groups crosslink the release coating composition together and permit the release coating to form a strong bond to the surface of the liner sheet. There are typically four levels of release force: premium release (10 to 15 g) , easy release (20 to 40 g) , high release (50 to lOOg) and tight release (>100 g) . For high speed label dispensing, the release liner should have a high release force. If the release force is too low, pre-dispensing occurs in which the labels disengage during die cutting rather than remain on the liner to form the roll stock.
Attempts to increase the release force by the addition of agents designed to strengthen the degree of release of the release coating cause unacceptable zippy noise, or zippiness, during matrix stripping and label dispensing. Zippy noise is an art-recognized term used to describe a jerking noise generated during the high speed matrix stripping process. This invention seeks to provide a release coating for use in high speed label dispensing machinery which does not cause pre-dispensing problems; for example, an unacceptable degree of zippy noise.
A feature of the invention is a release coating formulation which includes a mixture of (a) a silicone release component, (b) a crosslinking agent and (c) an acrylic ester.
According to one aspect of this invention, there is provided a flexible sheet, suitably but not exclusively for use as a release coated refuse liner, which has one one side thereof a crosslinkable release coating comprising a mixture of
(a) a material comprising a silicone moiety and plurality of unsaturated carboxylate groups;
(b) a crosslinking agent, differing from (a) , comprising a plurality of unsaturated carboxylate groups; and (c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) .
This invention also provides a crosslinkable release coating composition which comprises :
(a) a material comprising a silicone moiety and plurality of unsaturated carboxylate groups;
(b) a crosslinking agent, differing from (a) , comprising a plurality of unsaturated carboxylate groups; and
(c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) . This invention further provides a peelable adhesive film, for example a peelable label, which comprises a flexible sheet according to the invention and a face film stock releasably adhered by a tacky adhesive to the cured release coating.
Additionally, the present invention provides the use in a crosslinkable release coating composition which comprises :
(a) a material comprising a silicone moiety and plurality of unsaturated carboxylate groups;
(b) a crosslinking agent, differing from (a) , comprising a plurality of unsaturated carboxylate groups; and of (c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) to reduce pre-dispensing problems in high speed labelling.
An important feature of the invention is the use of a monomeric of oligomeric unsaturated carboxylic ester, preferably an acrylic ester in the release coating formulation. Suitable such acrylic esters are monomers or oligomers having long chain hydrocarbon groups. The hydrocarbon groups usually comprise 2 to 24 carbon atoms, specifically from 4 to 12 carbon atoms. Specific examples of contemplated acrylic esters include octyl acrylate, isodecyl acrylate, stearyl acrylate and lauryl acrylate. These materials have viscosity ranges from 2 to 55 cP (2 mPas to 55 mPas) at 25°C.
The film form liner is a conventional flexible film material known in this art. Examples of useful film form liner materials include paper, oriented polypropylene, polyethylene terephthalate, polyethylene, polyamides and polystyrene. The release coating is a composition which when applied to the base liner, has a low surface tack permitting ready release of other materials such as polymeric films which have been applied thereto.
The release coating formulation of this invention is, typically, crosslinkable and comprises a mixture of (a) a silicone release component; (b) a crosslinking agent; and (c) an acrylic ester.
In general, the (a) silicone release component is a polydimethyl siloxane silicone polymer which is known to have release characteristics. In general, the silicone polymers are themselves crosslinkable and have crosslinkable groups.
Crosslinkable silicone polymers of this kind usually have appended acrylic residues which are the crosslinkable groups. These crosslinkable silicone release polymers typically contain from 2%, such as 5%, to 30% acrylate, specifically from 10% to about 20% acrylate. An example of a typical release coating is a silicone-acrylate copolymer described in EPA 0281681. An example of a useful silicone-acrylate release polymer is available commercially under the name RC-726 by Goldschmidt Chemical Co.
In general the (b) crosslinking agent is present to permit bonding of the (a) silicone release component to the base liner. The crosslinking agent interacts with the acrylate by free radical reactions, typically, induced by high energy radiation, e.g. electron beam or ultra violet light. Conventional crosslinking agents can be employed in the release coating formulation. An example of a contemplated crosslinking agent is a higher acrylate content silicone-acrylate. The high acrylate content silicone-acrylate contemplated as the crosslinking agent is distinguished from the (a) silicone- acrylate by the presence of a higher concentration of the acrylate component. Typically, the (b) silicone-acrylate contains from 5 to 15% more acrylate than the (a) silicone- acrylate. Typically the high acrylate silicone-acrylate contains from 10% to 45%, more specifically from 15% to 30% acrylate based on the entire weight of this crosslinking agent. A high acrylate silicone-acrylate material, which contains about
25 % acrylate is sold commercially under the name RC-705 by Goldschmidt Chemical Co.
Other contemplated (b) crosslinking agents are multi- functionalized acrylate monomer/oligomer materials. Multi- functionalized acrylates are usually characterized by the presence of 2 or more acrylate groups per molecule. Examples include tri ethylolpropane triacrylate (TMPTA) and ethoxylated trimethylolpropane triacrylate (EO-TMPTA) . The TMPTA is sold under the name "SR-351" and the EO-TMPTA is sold under the name "SR-454", both sold by Sartomer Chemical Co. of Exton, PA.
The TMPTA and/or EO-TMPTA can be used together with the high acrylate silicone-acrylate crosslinking agent to make-up the appropriate amount of crosslinker needed in the release coating. Alternatively, the TMPTA and/or EO-TMPTA or the high acrylate silicone-acrylate can be used alone.
An important feature of this invention is the presence of a (c) acrylic ester in the release coating. The (c) acrylic ester when used with (a) and (b) to form a release coating has been found to produce a high release force release coating material. The (c) acrylic ester permits the above described (a) silicone release component to be used in high speed, high release force label applications. Prior to this invention, easy release force release coatings made from (a) silicone release components were unusable in high release force applications. It is believed that the addition of the (c) acrylic ester modifies the elastic property of the crosslinked silicone release coating.
Contemplated acrylic esters include monomeric and/or oligomeric acrylates. The acrylic esters contemplated are distinguished from the (a) and (b) silicone-acrylates described above by the absence of the silicone component. They are also distinguished from the (b) non-silicone crosslinking agent because they are usually free of more than two acrylate groups. Thus, more specifically, the acrylic ester can be defined as being free of silicone and free of more than 2 acrylate groups per molecule. Acrylic esters are derivatives of both acrylic acid and ethacrylic acid. The contemplated acrylates are specifically long chain alkyl esters containing 2 to 24 carbon atoms, the alkyl groups can be n-alkyl and secondary and branched chain alkyl groups. Typical examples of acrylic esters include octyl acrylate, isodecyl acrylate, stearyl acrylate and lauryl acrylate. Typically the acrylic esters have viscosity ranges from 2 to 55 cP at 25°C (2 mPas to 55 mPas) . These acrylic esters are commercially available from several chemical companies, such as Sartomer, UCB Radcure and CPS Chemicals. The release coating formulation is usually disposed on the base liner in an uncured from and is then cured to fix it in place. One of the techniques used to apply the release coating is to coat an uncured composition on a surface of the base liner and then to impinge an electron beam onto this composition for a time and under conditions suitable for converting this coating into a crosslinked film which is adhered to the surface of the base liner. Thus, the crosslinked release coating contains mostly crosslinked silicone acrylate moieties which are bound together and to the surface of the base liner. The coating can also be crosslinked by adding a UV initiator and then exposing the coating to UV light. Typical UV initiators are hydroquinone and hydroquinone derivatives.
The face stock is a conventional film form material. Examples of suitable materials are films of paper, oriented polypropylene, polyethylene terephthalate, polyethylene, polystyrene and metal foils. The adhesive is any material which will bond weakly to the release liner and strongly to the face stock. Examples of known adhesives include acrylic emulsions, such as those sold commercially under the name XPLA-12, by the Dyna-tech Company, styrene-butadiene rubber emulsions, such as those sold under the name Bond-master 72-9718 by National Starch Company, and hot- melt adhesives, such as those sold under the trade name HL-2021, or HL-2203X by the H.B. Fuller Company.
Included within the scope of this invention is a base liner provided with a skin of a material having tougher physical properties, adjacent to the release coating. This base liner is designed to facilitate label cutting. When the face stock, which is releasably secured to the release coating, is die cut into suitable shapes, the cutting die is prevented from penetrating and cutting through the base liner by the presence of the tougher skin layer.
The proportion of each component described above in the release coating formulation, based on the entire coating formulation, ranges from 15 to 70%, specifically from 20 to 50%, of the (a) silicone release component; from 10% to 50%, specifically from 15% to 30% of the (b) crosslinking agent; and from 10% to 50%, specifically from 20% to 40% of the (c) acrylic ester. The following Examples illustrate the invention; parts and percentages are by weight unless expressly stated. EXAMPLE 1
A release coating was formulated from a curable silicone- acrylate release component (RC-726 manufactured by Goldschmidt Chemical Co.), various proportions of the crosslinking agents, ethoxylated trimethylolpropane triacrylate (EO-TMPTA) and high acrylate silicone acrylate (HASA) , and isodecyl acrylate. The formulated release coating was coated onto a 2.0 mil oriented polypropylene film. After application of the release coating, the film was radiation cured by exposure to 2.5 Mrad electron beam radiation on an ESI Electrocurtain CB 150 laboratory EB unit. The release force of each coated release liner was tested by a TLMI tester. The TLMI tester is manufactured by TMI Co. , of Amityville, NY. In the test the sandwich laminate is cut into a 1 inch (25.4 mm) width. The face stock is peeled away at a 180° angle at a speed of 300 in/minute (1,270 mm/s) . The peel force is reported as the release force. The results are reported below in Table 1. The release liners were laminated to a high release force adhesive tape. The peel force at a speed of 3 and 5 meters per second was measured with IMASS tester. The IMASS tester is used to measure the release force for high speed operation. The tester used was model ZPE-1000, manufactured by Instrumentors, Inc., Strongsville OH which can be operated at speeds of 0.5 to 5.0 meters per second. The results are reported in Table 1.
Table 1
High Speed
Composition Peel Force
Release Zippy
Force (IMASS) noise
(TLMI) (IMASS
SAMPLE # 24 hr. test)
(g) isodecyl 3 m/s 5 m/s
10 SA1 HASA2 EO-TMPTA3 acrylate (g) (g)
1 50 50 30 25 13 no
2 30 70 35 30 20 no
3 50 20 30 88 57 38 no
15 4 67 13 20 64 84 58 no
5 33 27 40 98 73 62 slight
6 20 48 32 157 103 84 slight
7 35 39 26 78 104 80 no
8 50 30 20 105 159 108 slight
20 9 50 25 25 280 43 34 no
10 50 25 25 45 54 48 no
11 50 25 25 46 77 68 no
12 50 20 30 52 74 70 no
13 40 20 40 80 95 87 slight
25 14 55 15 30 55 75 51 no
SA = Silicone Acrylate _ HASA = High Acrylate Silicone Acrylate
EO-TMPTA = Ethoxylated Trimethylolpropane Triacrylate
EXAMPLE 2
Samples 1 to 8 were laminated to 60# high gloss paper face stock with a hot melt adhesive on a laboratory Mercer laminator. The laminates were then evaluated for their die cut performance on the Allied Gear FlexmasterlB die cut machine with a 3/4" circular die and the results are reported in Table 2. The percent predispense was determined by counting the number of labels predispensed during matrix stripping at 200 fpm (60.96 m/min) and 500 fpm (152.40 m/min) . TABLE 2
% Predispense at Zippiniess
Sample # During Matrix
(Table 1) 200 fpm 500 fpm Stripping
1 95 100 None
2 98 99 None
3 0 2 Slight
4 2 5 None 5 0 1 Moderate
6 0 1 Slight
7 5 10 None
8 0 3 Slight The data of Tables 1 and 2 show that release coating formulations made in accordance with this invention increase the release force of a silicone-acrylate release component and reduce the percentage of predispensed labels under high speed applications. The data reported in Table 1 show that silicone acrylate based release coatings formulated with a crosslinking agent, such as high acrylate silicone acrylate and/or ethoxylated trimethylolpropane triacrylate and an acrylate monomer achieve a high release force (>50 g) with only slight or no zippy noise. Varying the proportion of each component can optimize release coating performance. Additionally, as shown in Table 2, the amount of predispensed labels at high speeds is minimized by the use of the coating formulation of this invention.

Claims

1. A flexible sheet which has on one side thereof a crosslinkable release coating comprising a mixture of :
(a) a material comprising a silicone moiety and plurality of unsaturated carboxylate groups;
(b) a crosslinking agent, differing from (a) , comprising a plurality of unsaturated carboxylate groups; and
(c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) .
2. A flexible sheet according to claim 1 wherein, in (a) , the unsaturated carboxylate groups comprise from 2 to 30 wt.% of (a) of acrylate groups.
3. A flexible sheet according to claim 1 or 2 wherein (b) comprises (i) a silicone-acrylate material of higher acrylate content than (a) or (ii) a monomeric or oligomeric multi¬ functional acrylate.
4. A flexible sheet according to any preceding claim wherein (c) comprises a C2 to C24 alkyl acrylate monomer or oligomer.
5. A flexible sheet according to any preceding claim wherein (a) comprises from 15 to 70 wt.%; (b) comprises from 10 to 50 wt.%; and (c) comprises from 10 to 50 wt.% of the weight of the mixture.
6. A flexible sheet according to any preceding claim wherein the sheet comprises paper, polypropylene, polyethylene, polyethylene terephthalate, polyamide or polystyrene.
7. A flexible sheet according to any preceding claim for use as a release coated release liner.
8. A peelable adhesive film which comprises a flexible sheet according to any of claims 1 to 7 and a face film stock releasably adhered by a tacky adhesive to the cured release coating.
9. A crosslinkable release coating composition which comprises: (a) a material comprising a silicone moiety and plurality of unsaturated carboxylate groups;
(b) a crosslinking agent, differing from (a) , comprising a plurality of unsaturated carboxylate groups; and
(c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) .
10. Use in a crosslinkable release coating composition which comprises :
(a) a material comprising a silicone moiety and plurality of unsaturated carboxylate groups;
(b) a crosslinking agent, differing from (a) , comprising a plurality of unsaturated carboxylate groups; and of (c) a monomeric or oligomeric unsaturated carboxylic ester differing from (a) or (b) to reduce pre-dispensing problems in high speed labelling.
EP95910316A 1994-03-25 1995-02-22 Release sheet Withdrawn EP0751869A4 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/217,811 US5425991A (en) 1994-03-25 1994-03-25 Release sheet
US217811 1994-03-25
PCT/US1995/002175 WO1995026266A1 (en) 1994-03-25 1995-02-22 Release sheet

Publications (2)

Publication Number Publication Date
EP0751869A1 true EP0751869A1 (en) 1997-01-08
EP0751869A4 EP0751869A4 (en) 1998-04-15

Family

ID=22812632

Family Applications (1)

Application Number Title Priority Date Filing Date
EP95910316A Withdrawn EP0751869A4 (en) 1994-03-25 1995-02-22 Release sheet

Country Status (5)

Country Link
US (1) US5425991A (en)
EP (1) EP0751869A4 (en)
CA (1) CA2183582A1 (en)
SG (1) SG75766A1 (en)
WO (1) WO1995026266A1 (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6509077B1 (en) * 1995-11-01 2003-01-21 Moore Business Forms, Inc. Release coating for linerless labels, method of making a release coating and method of applying a release coating
US5932352A (en) * 1995-11-21 1999-08-03 Higgins; David Edward Release film
US5817376A (en) * 1996-03-26 1998-10-06 Minnesota Mining And Manufacturing Company Free-radically polymerizable compositions capable of being coated by electrostatic assistance
US5858545A (en) * 1996-03-26 1999-01-12 Minnesota Mining And Manufacturing Company Electrosprayable release coating
US5662985A (en) * 1996-05-21 1997-09-02 Mobil Oil Corporation Two-side coated label facestock
US6437015B2 (en) 1996-12-16 2002-08-20 Wacker-Chemie Gmbh Radiation-curing compositions
JP3417803B2 (en) * 1997-07-07 2003-06-16 リンテック株式会社 Hard coat sheet
US6150024A (en) * 1997-11-25 2000-11-21 Rexam Release, Inc. Acrylate release compositions and sheet materials having a release coating formed of the same
US6020412A (en) * 1997-12-04 2000-02-01 Mitsubishi Polyester Film, Llc Controlled release coating comprising blend of silicone polymer and adhesion promoter
US6723200B1 (en) 1999-08-18 2004-04-20 Meadwestvaco Corporation Method for releasing laminated materials
US6644395B1 (en) 1999-11-17 2003-11-11 Parker-Hannifin Corporation Thermal interface material having a zone-coated release linear
JP3760085B2 (en) * 2000-07-06 2006-03-29 リンテック株式会社 Process film for manufacturing ceramic green sheets
US20060165976A1 (en) * 2001-11-14 2006-07-27 Zuraw Paul J Release sheets for laminated materials
US20080017303A1 (en) * 2006-07-19 2008-01-24 Crouch Tarquin L Method and device for high speed labeling of articles using two-sided labelstock
DE102008059381A1 (en) * 2008-06-03 2009-12-17 Tesa Se Adhesive tape and its use
DE102009042008A1 (en) * 2009-09-21 2011-03-24 Huhtamaki Forchheim Zweigniederlassung Der Huhtamaki Deutschland Gmbh & Co. Kg Mainly biodegradable release film
US8758548B2 (en) * 2011-08-19 2014-06-24 Neenah Paper, Inc. Durable, heat resistant, erasable release coatings, release coated substrates, and their methods of manufacture
WO2013145864A1 (en) * 2012-03-28 2013-10-03 リンテック株式会社 Peeling film for step for producing ceramic green sheet
WO2016176525A1 (en) * 2015-04-29 2016-11-03 Avery Dennison Corporation Non-silicone additives in release coating materials

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2192400A (en) * 1986-07-07 1988-01-13 Kansai Paint Co Ltd Antifouling paint composition
EP0352339A1 (en) * 1987-07-02 1990-01-31 Toray Silicone Company, Limited Coating composition
WO1992016590A1 (en) * 1991-03-20 1992-10-01 Minnesota Mining And Manufacturing Company Radiation curable vinyl/silicone release coating

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4533566A (en) * 1984-07-05 1985-08-06 Minnesota Mining And Manufacturing Company Electron-beam adhesion-promoting treatment of polyester film base for silicone release liners
US4786552A (en) * 1986-07-07 1988-11-22 Avery International Corporation Curable arcylic/fumaric pressure-sensitive adhesives
MY103125A (en) * 1987-07-24 1993-04-30 Lintec Corp Cover tape for sealing chip-holding parts of carrier tape
US5234736A (en) * 1989-02-24 1993-08-10 Avery Dennison Corporation Stock for labels and tapes utilizing siliconized emulsion based pressure-sensitive adhesives
US4994538A (en) * 1989-02-24 1991-02-19 Avery International Corporation Siliconized emulsion based pressure-sensitive adhesives
JP3007121B2 (en) * 1990-08-02 2000-02-07 東レ・ダウコーニング・シリコーン株式会社 Organopolysiloxane-acrylate copolymer emulsion
US5194501A (en) * 1990-10-30 1993-03-16 Minnesota Mining And Manufacturing Company Pressure-sensitive adhesive based on ethylenically-unsaturated α-olefin polymer cured with hydrosilane
US5242726A (en) * 1991-09-23 1993-09-07 Minnesota Mining And Manufacturing Company Pattern-coated anchorage system for porous film
US5246756A (en) * 1992-01-29 1993-09-21 Mobil Oil Corporation Release sheet
US5248535A (en) * 1992-01-29 1993-09-28 Mobil Oil Corporation Release sheet

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2192400A (en) * 1986-07-07 1988-01-13 Kansai Paint Co Ltd Antifouling paint composition
EP0352339A1 (en) * 1987-07-02 1990-01-31 Toray Silicone Company, Limited Coating composition
WO1992016590A1 (en) * 1991-03-20 1992-10-01 Minnesota Mining And Manufacturing Company Radiation curable vinyl/silicone release coating

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9526266A1 *

Also Published As

Publication number Publication date
SG75766A1 (en) 2000-10-24
US5425991A (en) 1995-06-20
WO1995026266A1 (en) 1995-10-05
EP0751869A4 (en) 1998-04-15
CA2183582A1 (en) 1995-10-05

Similar Documents

Publication Publication Date Title
US5425991A (en) Release sheet
US6218006B1 (en) Pressure-sensitive adhesive composition and pressure-sensitive adhesive sheets made therefrom, and sealants, reinforcing sheets and pressure-sensitive adhesive sheets for printing produced therefrom
US6492019B1 (en) Activated adhesive system
US5654093A (en) Release-coated articles and multilayer articles containing same
CA2114466C (en) Radiation curable hot melt pressure sensitive adhesives
US5436073A (en) Multi-layer composite
EP1160301B1 (en) Pressure-sensitive adhesive composition curable with actinic energy ray and pressure-sensitive adhesive sheet
US5543231A (en) Radiation-curable silicone release compositions
EP0902071A1 (en) Thermosetting pressure-sensitive adhesive and adhesive sheets made by using the same
JP2000109770A (en) Production of adhesive sheet and adhesive sheet
US5562992A (en) Radiation-curable silicone release compositions and coated articles
JP3078362B2 (en) Radiation-curable adhesive and its adhesive tape
JP2596707B2 (en) Radiation curable hot melt pressure sensitive adhesive
JPH10251609A (en) Self-adhesive composition and peelable self-adhesive tape or sheet
JP2005023114A (en) Pressure-sensitive type double-sided adhesive tape or sheet
JPH1025459A (en) Pressure-sensitive adhesive composition
US7056408B2 (en) High performance adhesive
EP1164886B1 (en) Loop fastening material
WO2023176023A1 (en) Adhesive sheet and method for manufacturing adhesive sheet
JP2001172578A (en) Pressure sensitive adhesive sheet
JP2897015B2 (en) Manufacturing method of laminate
WO2023012947A1 (en) Adhesive sheet and adhesive sheet manufacturing method
DE69635799T2 (en) PRESSURE-RESISTANT ADHESIVE COMPOSITION AND PRINT-SENSITIVE ADHESIVES AND SEAL MASSES, IMPRESSION FOILS, AND PRESSURE-SENSITIVE ADHESIVE PRINTED FOILS MANUFACTURED THEREFROM
JPH0820749A (en) Radiation-curing pressure-sensitive adhesive composition and pressure-sensitive adhesive tape or sheet coated therewith
JP2001098226A (en) Uv-curable pressure-sensitive adhesive and pressure- sensitive adhesive sheet using the same

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19960813

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE ES FR GB IT NL

A4 Supplementary search report drawn up and despatched

Effective date: 19980304

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): BE DE ES FR GB IT NL

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: EXXONMOBIL OIL CORPORATION

17Q First examination report despatched

Effective date: 20020206

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20020618